Metoprolol Succinate ER

Product NDC: 51655-573
11-digit product format: 516550573
Labeler code: 51655
Product ID: 51655-573_4d382c97-704e-1603-e054-00144ff8d46c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Metoprolol Succinate ER
Dosage form: TABLET, EXTENDED RELEASE
Route: ORAL
Labeler: Northwind Pharmaceuticals
Application: ANDA078889
Marketing category: ANDA
Marketing start: 2016-04-07
Marketing end: 0000-00-00
Substance: METOPROLOL SUCCINATE
Active strength: 100 mg/1
Pharmacologic classes: Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag: No
Listing certified through: 2019-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-573-52	2026-01-09	C162847	48780-1	9d75b9d0-82b4-f424-e053-dadaa90a57ce	4d382c97-704d-1603-e054-00144ff8d46c
51655-573-52	2020-01-31	C162847	48780-1	9d75b9d0-82b4-f424-e053-dadaa90a57ce	4d382c97-704d-1603-e054-00144ff8d46c

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-573	METOPROLOL SUCCINATE ER TABLET, EXTENDED RELEASE [NORTHWIND PHARMACEUTICALS]	1	Legacy NDC	20170415_4d382c97-704d-1603-e054-00144ff8d46c.zip